US20060035798A1 - Non-aqueous water and oil repellent compositions for a durable hydrophobic textile - Google Patents
Non-aqueous water and oil repellent compositions for a durable hydrophobic textile Download PDFInfo
- Publication number
- US20060035798A1 US20060035798A1 US11/254,201 US25420105A US2006035798A1 US 20060035798 A1 US20060035798 A1 US 20060035798A1 US 25420105 A US25420105 A US 25420105A US 2006035798 A1 US2006035798 A1 US 2006035798A1
- Authority
- US
- United States
- Prior art keywords
- sub
- component
- group
- fluorine
- oil repellent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 239000004753 textile Substances 0.000 title claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 17
- 230000002940 repellent Effects 0.000 title claims 11
- 239000005871 repellent Substances 0.000 title claims 11
- 230000002209 hydrophobic effect Effects 0.000 title claims 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 18
- 239000011737 fluorine Substances 0.000 claims abstract description 18
- 238000004381 surface treatment Methods 0.000 claims abstract description 9
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- RIQRGMUSBYGDBL-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,5-decafluoropentane Chemical compound FC(F)(F)C(F)C(F)C(F)(F)C(F)(F)F RIQRGMUSBYGDBL-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 239000004606 Fillers/Extenders Substances 0.000 claims description 3
- 239000004599 antimicrobial Substances 0.000 claims description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical class O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims description 2
- 239000011521 glass Substances 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims 15
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 229920000642 polymer Polymers 0.000 claims 8
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 4
- 239000012948 isocyanate Substances 0.000 claims 4
- 229910052709 silver Inorganic materials 0.000 claims 4
- 239000004332 silver Substances 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- -1 acetylene alcohols Chemical class 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 150000002894 organic compounds Chemical class 0.000 claims 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims 2
- 239000004593 Epoxy Substances 0.000 claims 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 238000004132 cross linking Methods 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- 150000002513 isocyanates Chemical class 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical group Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 239000001993 wax Substances 0.000 claims 2
- 239000010457 zeolite Substances 0.000 claims 2
- XFNJYAKDBJUJAJ-UHFFFAOYSA-N 1,2-dibromopropane Chemical compound CC(Br)CBr XFNJYAKDBJUJAJ-UHFFFAOYSA-N 0.000 claims 1
- GDMDOMRUYVLLHM-UHFFFAOYSA-N 2-(1-iodoethyl)pentyl carbamate Chemical compound CCCC(C(C)I)COC(N)=O GDMDOMRUYVLLHM-UHFFFAOYSA-N 0.000 claims 1
- CYXIKYKBLDZZNW-UHFFFAOYSA-N 2-Chloro-1,1,1-trifluoroethane Chemical group FC(F)(F)CCl CYXIKYKBLDZZNW-UHFFFAOYSA-N 0.000 claims 1
- NAMYKGVDVNBCFQ-UHFFFAOYSA-N 2-bromopropane Chemical compound CC(C)Br NAMYKGVDVNBCFQ-UHFFFAOYSA-N 0.000 claims 1
- MGQSMKJLJXWTEH-UHFFFAOYSA-N 3-butyl-1,2-benzothiazole Chemical compound C1=CC=C2C(CCCC)=NSC2=C1 MGQSMKJLJXWTEH-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- KSQXVLVXUFHGJQ-UHFFFAOYSA-M Sodium ortho-phenylphenate Chemical compound [Na+].[O-]C1=CC=CC=C1C1=CC=CC=C1 KSQXVLVXUFHGJQ-UHFFFAOYSA-M 0.000 claims 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 claims 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 claims 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 claims 1
- 150000001241 acetals Chemical class 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 claims 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 125000005442 diisocyanate group Chemical class 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000004991 fluoroalkenyl group Chemical group 0.000 claims 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 238000005342 ion exchange Methods 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 229910000000 metal hydroxide Inorganic materials 0.000 claims 1
- 150000004692 metal hydroxides Chemical class 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 125000004971 nitroalkyl group Chemical group 0.000 claims 1
- 150000004812 organic fluorine compounds Chemical class 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 150000008301 phosphite esters Chemical class 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 claims 1
- 229960002026 pyrithione Drugs 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 235000010294 sodium orthophenyl phenol Nutrition 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 229910001428 transition metal ion Inorganic materials 0.000 claims 1
- 150000003852 triazoles Chemical class 0.000 claims 1
- 229960003500 triclosan Drugs 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Chemical class 0.000 claims 1
- 239000011787 zinc oxide Substances 0.000 claims 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003063 flame retardant Substances 0.000 abstract description 2
- 238000005265 energy consumption Methods 0.000 abstract 1
- 238000010792 warming Methods 0.000 abstract 1
- 239000000758 substrate Substances 0.000 description 25
- 238000011282 treatment Methods 0.000 description 13
- 238000012360 testing method Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 8
- 239000006260 foam Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000002964 rayon Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 239000004088 foaming agent Substances 0.000 description 4
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 2
- 101100352919 Caenorhabditis elegans ppm-2 gene Proteins 0.000 description 2
- 239000008365 aqueous carrier Substances 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000004758 synthetic textile Substances 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- WBHAUHHMPXBZCQ-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound COC1=CC=CC(C)=C1O WBHAUHHMPXBZCQ-UHFFFAOYSA-N 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004855 creaseproofing Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical class FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/08—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with halogenated hydrocarbons
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B9/00—Solvent-treatment of textile materials
- D06B9/06—Solvent-treatment of textile materials with recovery of the solvent
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/10—Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/11—Oleophobic properties
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/12—Hydrophobic properties
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
- Y02P70/62—Manufacturing or production processes characterised by the final manufactured product related technologies for production or treatment of textile or flexible materials or products thereof, including footwear
Definitions
- Fluoro-chemicals are now applied to substrates via application with water based (aqueous) carriers requiring other auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
- auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
- chlorinated hydrocarbons have been used in the past as carrier mediums to apply organic chemicals to substrates when an aqueous carrier could not be used. Most chlorinated hydrocarbons are being phased out by mandate of the Environmental Protection Agency (EPA).
- EPA Environmental Protection Agency
- Chlorofluorocarbons have been widely used as solvents for solvent-based fluorine-containing surface treatment compositions because the chlorofluorocarbons are less toxic, nonflammable and chemically stable.
- Particularly CFC-113 which has a moderate boiling point, has been widely used.
- ozone layer depletion by specific chlorofluorocarbons such as CFC-113 became a problem and production of such chlorofluorocarbons has been discontinued on a world-wide scale.
- NPB n-propyl bromide
- 2,3-dihydrodeca-fluoropentane have shown to be a excellent alternatives to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates. Both are examples of a non-regulated, non-toxic alternatives with little to no ozone pollution properties. NPB is very economical and environmentally friendly.
- NPB NPB
- the invention relates to non-aqueous surface treatments to provide substrates oil and water repellant.
- the treatment of home textiles and apparel which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as compared to available current technology, illustrated in Example 2 Compared to Example 4.
- compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements.
- Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably no heat treatment being necessary (Example 3).
- invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment.
- other textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently.
- additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, urethane, finishing agents, extenders and antimicrobials for textile auxiliaries and others.
- Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard.
- Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
- compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
- Textiles as base substrates, preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process.
- the padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2).
- the textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off.
- the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used.
- the spraying process (Example 3) the textile is sprayed with the treatment liquor.
- the treatment liquor is finely divided by nozzles and applied uniformly. An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
- the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent.
- the foam is produced in the mixing head by mixing the liquor with air.
- the foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator.
- the goods are pressed against the slot and taken off via a separate unit, for example a stenter frame.
- a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used.
- the experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
- this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
- the textiles preferably home textiles
- the textiles are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure.
- good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
- Oil-repellency (according to AATCC 118-1972): The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
- the AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds.
- the test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
- Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample.
- the test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
- compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E.I. Dupont)
- compositions according to the invention are non-aqueous solutions contents of which comprise a mixture of NPB or 2,3-dihydrodeca-fluoropentane (component A) and one or more poly (meth) acrylates (component B).
- the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The object of the invention is to provide a fluorine-containing non-aqueous surface treatment composition for application by current commercially available equipment that has, excellent performance, a long shelf life, reduced energy consumption, very little to no ozone layer depletion and global warming. and is highly safe due to the non-flammability or flame retardant characteristics.
Description
- This application is a continuation in part of patent application Ser. No. 10/611,746, Filed Jun. 30, 2003, Titled “Chemical formulations and methods utilizing NPB (n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates”
- Fluoro-chemicals are now applied to substrates via application with water based (aqueous) carriers requiring other auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
- These auxiliary chemicals needed for aqueous application often lesson the intended benefit of the applied chemical to the substrate. Aqueous chemistries require high curing temperatures and expensive drying systems to evaporate the water. Chlorinated hydrocarbons have been used in the past as carrier mediums to apply organic chemicals to substrates when an aqueous carrier could not be used. Most chlorinated hydrocarbons are being phased out by mandate of the Environmental Protection Agency (EPA).
- Chlorofluorocarbons have been widely used as solvents for solvent-based fluorine-containing surface treatment compositions because the chlorofluorocarbons are less toxic, nonflammable and chemically stable. Particularly CFC-113, which has a moderate boiling point, has been widely used. However, ozone layer depletion by specific chlorofluorocarbons such as CFC-113 became a problem and production of such chlorofluorocarbons has been discontinued on a world-wide scale.
- By this invention, NPB (n-propyl bromide) and 2,3-dihydrodeca-fluoropentane have shown to be a excellent alternatives to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates. Both are examples of a non-regulated, non-toxic alternatives with little to no ozone pollution properties. NPB is very economical and environmentally friendly.
- After extensive study, it has been found that the use of NPB as a carrier for application dramatically improves the performances and durability of textiles and that this invention is superior to current methods and chemistry being applied by foam.
- The invention relates to non-aqueous surface treatments to provide substrates oil and water repellant. As example, the treatment of home textiles and apparel, which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as compared to available current technology, illustrated in Example 2 Compared to Example 4.
- The following description, taken in conjunction with the referenced examples, is presented to enable one of ordinary skill in the art to make and use the invention. Various modifications will be readily apparent to those Skilled in the art, and the general principles defined herein may be applied to a wide range of aspects. Thus, the present invention is not intended to be limited to the aspects presented, but is to be accorded the widest scope consistent with the principles and novel features disclosed herein. Furthermore, the compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements.
- Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably no heat treatment being necessary (Example 3).
- In one aspect, invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment. In another aspect, other textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently. Such additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, urethane, finishing agents, extenders and antimicrobials for textile auxiliaries and others.
- Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard. Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
- Processes for the treatment of such base substrates and therefore for application of the fluorine-containing compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
- Textiles as base substrates, preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process. The padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2). The textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off. In the padding process, the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used. In the spraying process, (Example 3) the textile is sprayed with the treatment liquor. The treatment liquor is finely divided by nozzles and applied uniformly. An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
- In the foaming process, the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent. The foam is produced in the mixing head by mixing the liquor with air. The foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator. The goods are pressed against the slot and taken off via a separate unit, for example a stenter frame. In example 1, a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used. The experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
- By the invention, it has been discovered surprisingly that mixtures of NPB and Perfluoroalkyl polyacrylate can be foamed with or without the aid of a foaming agent (Example 1). Not using foaming agents greatly improves the benefit of the applied fluorine composition to the substrate and reduces the amount of compound added to fabric to achieve water and oil repellency. In another aspect, this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
- After the treatment, the textiles, preferably home textiles, are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure. However, good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
- Samples of the materials thus pretreated were taken for testing of the following effects:
- Oil-repellency (according to AATCC 118-1972): The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
- The AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds. The test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
- Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample. The test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
- Compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E.I. Dupont)
- The compositions according to the invention (Examples 1, 2 & 3) are non-aqueous solutions contents of which comprise a mixture of NPB or 2,3-dihydrodeca-fluoropentane (component A) and one or more poly (meth) acrylates (component B).
- A solution of 98% NPB and 2% Perfluoroalkyl polyacrylate were mixed and applied to the foam generator which imparts the solution to a high speed mixer that generates the solution into foam. The foam was then dispensed to the substrates listed in below via an applicator at 30%-wet pickup. The substrates were then dried at 170 deg C. for 1-minute dwell time with the following results:
Initial After 10 Home Laundries Example 1 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 5 85 100 2160 ppm 2 60 70 1600 ppm Polyester 6 90 100 1170 ppm 5 90 90 980 ppm Pes/Rayon 6 80 100 5 60 70 - A solution of 99.6% NPB and 0.4% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a pad applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
Initial After 10 Home Laundries Example 2 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 6 100 100 2480 ppm 3 90 80 2200 ppm Polyester 8 90 100 1270 ppm 6 90 90 1100 ppm Pes/Rayon 8 80 100 6 8O 80 - A solution of 99.6% 2,3-dihydrodeca-fluoropentane and 0.4% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a Spray at 1.5 bars pressure. The solution was applied at noted wet pickup. The substrates were air dried at room temperature.
Initial After 10 Home Laundries Example 3 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 6 85 100 2260 ppm 2 4O 60 1370 ppm Polyester 7 90 10O 1170 ppm 3 90 70 1080 ppm Pes/Rayon 6 80 100 3 60 60 - An aqueous Perfluoroalkyl polyacrylate dispersion using Nuva HPU at 2% concentration was prepared and applied via a padding applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
Initial After 10 Home Laundries Example 4 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 7 100 100 2460 7 90 80 2210 ppm ppm Polyester 6 60 100 1270 4-5 45-50 90 1100 ppm ppm Pes/Rayon 5 60 100 2 35-40 70 - In all examples, the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.
Claims (13)
1. A non-aqueous water and oil repellent composition for a durable hydrophobic textile comprising:
(A) a fluorine-containing polymer or copolymer component,
(B) a solvent component,
(C) a cross-linking or extender component.
2. A Water and oil repellent composition according to claim 1 , wherein the fluorine containing component (A) is a surface treatment component and comprises at least one species selected from the group consisting of: (1) phosphorus-containing compounds having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups; (2) highly fluorinated organic compounds; and (3) polymers prepared using, as a monomer component, a compound having a at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups, said highly fluorinated organic compound (2) being at least one compound selected from the group consisting of:
(A) at least one fluoroalkane selected from the group consisting of (CF.sub.3).sub.2 CF(CF.sub.2).sub.4 CF(CF.sub.3).sub.2 and ##STR36##
(B) at least one fluorochloro polyether selected from the group consisting of: F(CHClCF.sub.2 CF.sub.2 O).sub.n CHClCF.sub.3 (n is 5 on an average); F(CCl.sub.2 CF.sub.2 CF.sub.2 O).sub.n CCl.sub.2 CF.sub.3 (n is 5 on an average); F(CCl.sub.2 CF.sub.2 CF.sub.2 O). sub.n CCl.sub.2 CF.sub.2 Cl (n is 25 on an average); CCl.sub.2 FCF.sub.2 CF.sub.2 OCCl.sub.2 CF.sub.2 CF.sub.2 OCCl.sub.2 CF.sub.3; F(CCl.sub.x F.sub.y CF.sub.2 CF.sub.2 O).sub.n CCl.sub.x F.sub.y CF.sub.3 (n is 5 on an average), x+y=2, x:y=1:4); F(CF.sub.2 CF.sub.2 CF.sub.2 O).sub.x (CClFCF.sub.2 CF.sub.2 O).sub.y —CF.sub.2 CF.sub.2 COF (x+y is 20 on an average, x:y=2:1, x number of units and y number of units are arranged in a random order); and F(CF.sub.2 CF.sub.2 CF.sub.2 O).sub.x (CClFCF.sub.2 CF.sub.2 O).sub.y CF.sub.2 CF.sub.3 (x+y is 20 on an average, x:y=2:1, x number of units and y number of units are arranged in a random order), and
(C) fluorochloroolefin telomers whose main portion, defined as a portion except for terminal groups, is composed of repeating units of —CF.sub.2 CFCl—, the total of the repeating units of chlorotrifluoroethane in terms of degree of telomerization being 3 to 20, and said polymer (3) prepared using as, a monomer component, a compound having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups being at least one polymer selected from the group consisting of:
(A) a copolymer of at least one fluorine-containing monomer selected from the group consisting of polyfluoroalkyl-containing (meth)acrylic esters, polyfluoroalkenyl-containing (meth)acrylic esters, polyfluoroalkyl-containing vinyl compounds and poly-fluoroalkenyl-containing vinyl compounds, and another monomer copolymerizable therewith, the proportion of the fluorine-containing monomer being 20-95 parts by weight, based on 100 parts by weight of the total monomer component, and
(B) a polymer of at least one fluorine-containing monomer selected from the group consisting of polyfluoroalkyl-containing epoxy monomers and polyfluoroalkenyl-containing epoxy monomers, or a copolymer of the fluorine-containing monomer and another monomer copolymerizable therewith, the proportion of the fluorine-containing monomer being 20-100 parts by weight, based on 100 parts by weight of the total monomer component.
3. A Water and oil repellent composition according to claim 1 , wherein the fluorine containing component (A) is a surface treatment component comprising a polymer prepared using as a monomer component having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups.
4. A Water and oil repellent composition according to claim 1 , wherein the solvent component (B) is stabilized. wherein said stabilizer (or corrosion inhibitor) is selected from the group consisting of alkanols having 4 to 7 carbon atoms, nitroalkanes having 1 to 3 carbon atoms, 1,2-epoxyalkanes having 2 to 7 carbon atoms, acetylene alcohols having 3 to 9 carbon atoms, phosphite esters having 12 to 30 carbon atoms, ethers having 3 to 6 carbon atoms, unsaturated hydrocarbon compounds having 4 to 7 carbon atoms, triazoles, acetals having 4 to 7 carbon atoms, ketones having 3 to 5 carbon atoms, amines having 6 to 8 carbon atoms, and mixtures thereof.
5. A Water and oil repellent composition according to claim 1 , wherein the solvent component (B) is a bromine-containing solvent and is a C.sub. 1-3 alogenated hydrocarbon having at least one bromine atom.
6. A water and oil repellent composition according to claim 1 , wherein the solvent component (B) is a bromine-containing solvent with at least one compound selected from the group consisting of 1-bromopropane, 2-bromopropane and 1,2-dibromopropane
7. A Water and oil repellent composition according to claim 1 , wherein the solvent component (B) is selected from the group consisting of: 2,3-dihydrodeca-fluoropentane, mixture of 2,3-dihydrodeca-fluoropentane and trans-1,2-dichloroethylene, mixture of 2,3-dihydrodeca-fluoropentane and trans-1,2-dichloroethylene with cyclopentane.
8. A Water and oil repellent composition according to claim 1 , wherein the cross-linking or extender component (C), is selected from the group comprising one or more of the following: melamine formaldehyde derivatives, trimethylolmelamine, hexamethylolmelamine, epoxides, anhydrides and derivatives thereof.
Derivatives of isocyanates, diisocyanates. Polymers containing two or more blocked isocyanate compounds or aromatic blocked isocyanates. Monomers or polymers containing isocyanate compounds, zirconium tetra-butanolate, paraffine waxes, microcrystalline or semicrystalline waxes and melamine-paraffin waxes, whereas said component (C) is 0.001% to 60% by weight of component B.
9. A Water and oil repellent composition according to claim 1 , which further contains (D), which is an antibacterial component comprising one or more organic antimicrobial agents to include: Silver containing resins, silver containing zeolites, silver containing glass, silver based ion exchange compounds, triclosan and inorganic antimicrobial materials: metal based zeolites, metal salts, metal oxides, metal hydroxides, transition metal ions, zinc oxide, pyrithione containing materials, tributyl oxides derivatives, 3-iodo-2 propyl butyl carbamate, n-butyl-1,2 benzisothiazoline, 10,10′-oxybisphenoxi arsine, sodium o-phenylphenate, whereby component (D) is 0.001% to 5% by weight of component (A).
10. A process for surface treatment of an article to be treated, which comprises treating the textile with the surface treatment compositions according to claim 1 , followed by drying and curing.
11. A process for surface treatment of an article to be treated, which comprises treating the textile with the surface treatment compositions according to claim 9 , followed by drying and curing.
12. A textile which is treated with the water and oil repellent compositions according to claim 1 .
13. A textile which is treated with the compositions according to claim 9.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/254,201 US20060035798A1 (en) | 2003-06-30 | 2005-10-20 | Non-aqueous water and oil repellent compositions for a durable hydrophobic textile |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/611,746 US20040006827A1 (en) | 2002-07-03 | 2003-06-30 | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
| US11/254,201 US20060035798A1 (en) | 2003-06-30 | 2005-10-20 | Non-aqueous water and oil repellent compositions for a durable hydrophobic textile |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/611,746 Continuation-In-Part US20040006827A1 (en) | 2002-07-03 | 2003-06-30 | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
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| Publication Number | Publication Date |
|---|---|
| US20060035798A1 true US20060035798A1 (en) | 2006-02-16 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/254,201 Abandoned US20060035798A1 (en) | 2003-06-30 | 2005-10-20 | Non-aqueous water and oil repellent compositions for a durable hydrophobic textile |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7842625B1 (en) | 2006-10-26 | 2010-11-30 | Nano-Tex, Inc. | Methods for treating fabric to facilitate moisture transfer from one side to the other |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637614A (en) * | 1969-02-27 | 1972-01-25 | Du Pont | Solvent soluble dry soil resistant fluoropolymers |
| US3657173A (en) * | 1969-03-03 | 1972-04-18 | Du Pont | Oil and water repellent compositions |
| US6120892A (en) * | 1997-11-20 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Waterborne fluoropolymer solutions for treating hard surfaces |
| US20030224112A1 (en) * | 2002-06-03 | 2003-12-04 | 3M Innovative Properties Company | Fluorochemical composition and method of treatment of a substrate therewith to render substrate oil-and/or water repellent |
| US7435774B2 (en) * | 2002-09-11 | 2008-10-14 | Peach State Labs, Inc. | Fluoromonomers, fluoropolymers, methods of preparing them, and their application to various surfaces and substrates |
-
2005
- 2005-10-20 US US11/254,201 patent/US20060035798A1/en not_active Abandoned
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637614A (en) * | 1969-02-27 | 1972-01-25 | Du Pont | Solvent soluble dry soil resistant fluoropolymers |
| US3657173A (en) * | 1969-03-03 | 1972-04-18 | Du Pont | Oil and water repellent compositions |
| US6120892A (en) * | 1997-11-20 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Waterborne fluoropolymer solutions for treating hard surfaces |
| US20030224112A1 (en) * | 2002-06-03 | 2003-12-04 | 3M Innovative Properties Company | Fluorochemical composition and method of treatment of a substrate therewith to render substrate oil-and/or water repellent |
| US7435774B2 (en) * | 2002-09-11 | 2008-10-14 | Peach State Labs, Inc. | Fluoromonomers, fluoropolymers, methods of preparing them, and their application to various surfaces and substrates |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7842625B1 (en) | 2006-10-26 | 2010-11-30 | Nano-Tex, Inc. | Methods for treating fabric to facilitate moisture transfer from one side to the other |
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